Quality Assurance Intern-Memphis, TN *Spring 2023* (EG)
Charles River Laboratories International Inc (CRL)
Memphis, TN, US, 38118
Quality Assurance Intern-Memphis, TN *Spring 2023* (EG) Req ID #: 196591 Location:
Memphis, TN, US, 38118 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly. Job Summary
Must be willing to work on-site (Memphis, TN) and be willing to dedicate 16 hours per week with your upcoming Spring 2023 semester.
We are seeking a Quality Assurance Intern for our Cell Therapy Manufacturing Facility located in Memphis, TN.
The Quality Assurance Intern is responsible for successfully completing the internship program course leading up to the potential involvement of various Quality Assurance related activities associated with the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to meet physical requirements established in this job description.
The following are responsibilities related to the Quality Assurance Intern:
• Complete training necessary for the performance of aseptic activities.
• Consistently practice appropriate clean room behaviors.
• Demonstrate necessary knowledge of cGMP requirements.
• Obtain detailed knowledge of 21 CFR Part 11 compliance as it pertains to Quality Assurance.
• Display an ability to create and review cGMP documentation.
• Demonstrates strong verbal and written communication skills.
• Display an ability to think critically and assess risk.
• Perform other duties as assigned. Job Qualifications
The following are minimum qualifications related to the Quality Assurance Intern position:
• Currently enrolled in a Bachelor or Associate’s program with a preferred minimum of 3.0 GPA.
• Must be detailed oriented and have excellent organizational skills.
• Must possess effective written and oral communication skills.
• Must display a high degree of professionalism and confidentiality.
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19. Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees.
Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition ([email protected]) so that information can be provided about the accommodation process at Charles River.
About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to [email protected] This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
Nearest Major Market: Memphis
Job Segment: Pharmaceutical, Quality Assurance, Recruiting, Telecom, Telecommunications, Science, Technology, Human Resources
Similar CRA jobs
Senior Scientist - Small Molecule HPLC , Quality Control , GMP
Senior Quality Manager TQM
Sr. Director Quality Assurance
Clinical Quality Operations Manager (FSP)
Sr. Quality Assurance Auditor - GMP
Group Leader - Quality Control Lab - Biopharma
Quality Assurance Auditor (Sherbrooke)
Quality Control Associate - Lab Sciences **$1000 Sign on Bonus 1
Technology Quality Specialist
Senior Quality Assurance Auditor / GCP監査
Operation Quality Management Specialist
Quality Laboratory Coordinator
Senior Quality Assurance Engineer - Team Lead
Orthopedic Specialist Representative (Wound Closure & Biosurgery) – Medical Device Sales - St Louis E , MO - Springfield/Mt Vernon, IL - UYA26743
Quality Assurance Assistant (Part time)
Pharmaceutical Sales Representative - Springfield, MO - 2594856
Data Analyst 1 - Quality Control
Supervisor - Quality Control
Senior Scientist - Quality Control Testing
Quality Assurance Specialist III